HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 443794Generated: October 30, 2026
Water → 7-chloro-3-dipropylacetoxy-5-(2'-fluorophenyl)-1,3-dihydro-2H-1,4-benzodiazepine-2-one
https://huagongshe.com/reaction/443794
Participants
| Role | Name | HCID | Charge |
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| Reactant | Water | HCID 962 | — |
| Reactant | 2-Propylpentanoyl 2-propylpentanoate | HCID 10923624 | — |
| Reactant | Acetone cyclohexane | HCID 21916603 | — |
| Reactant | HCID 178516821 | HCID 178516821 | — |
| Solvent | Chloroform | HCID 6212 | — |
| Product | 7-chloro-3-dipropylacetoxy-5-(2'-fluorophenyl)-1,3-dihydro-2H-1,4-benzodiazepine-2-one | HCID 23465565 | — |
Reaction Steps
A suspension of 10 g of 7-chloro-5-(2'-fluoro-phenyl)-1,3-dihydro-2H-1,4-benzodiazepine-2-one-4-oxide in 20 ml of absolute chloroform is mixed with 14.3 g of dipropyl acetic acid anhydride and is heated under reflux and with the exclusion of atmospheric moisture for such a length of time until a sample on the thin layer-chromatogram (silica gel 60 F 254 of the firm Merck, flow agent: cyclohexane/acetone=1:1) shows a complete conversion. Then, the cooled mixture is shaken out several times with water, the organic phase is dried with Na2SO4 and the filtrate is evaporated in the vacuum. Upon standing over night, the residue crystallizes, is washed with petroleum ether and recrystallized from aceontrile. One will obtain a colorless powder of 7-chloro-3-dipropylacetoxy-5-(2'-fluorophenyl)-1,3-dihydro-2H-1,4-benzodiazepine-2-one, which melts at 147°-149°.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US04261987 |
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| Source dataset | uspto-grants-1981_04 |
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| ORD ID | ord-7a5b95c8da074024975d6528edeb2885 |
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| Source note | uspto-grants-1981_04 |
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